What are the early signs of Parkinson’s Disease?

The early signs of Parkinson’s disease often appear subtly and may go unnoticed at first. A common early indicator is a mild hand tremor that occurs at rest. Other early symptoms include smaller handwriting, slower movement, a soft or muffled voice, reduced facial expressions (sometimes called “masked face”), and difficulty with balance or coordination.Some people also notice changes in posture or experience unexplained stiffness in their limbs. These signs may vary from person to person and tend to develop gradually. Early recognition is important, as it can lead to a timely diagnosis and the start of symptom management.While these signs don’t confirm a diagnosis on their own, they serve as important clues for medical professionals evaluating the presence of Parkinson’s Disease in its initial stages.

How many stages are there in Parkinson’s Disease, and how are they treated?

Treatment across stages varies but often includes medication (such as Levodopa), physical therapy, occupational therapy, and, in some cases, deep brain stimulation. Managing symptoms early can slow progression, and personalized care plans are key.Understanding these stages helps patients and caregivers prepare for evolving challenges while maximizing independence.

Can Parkinson’s Disease be inherited?

While most cases of Parkinson’s Disease are considered sporadic (not inherited), approximately 10–15% are linked to genetic mutations. These inherited forms are often associated with specific genes such as LRRK2, PARK7, PINK1, and SNCA. In some families, these mutations are passed from generation to generation, increasing the risk of developing the condition, especially in younger individuals with early-onset Parkinson’s. However, having a mutation does not guarantee a diagnosis; it simply raises the probability. Environmental triggers may also interact with genetic predispositions to initiate the disease. Genetic testing is available for certain mutations, though it’s typically recommended only in specific cases with a strong family history.While Parkinson’s Disease can be inherited, most people diagnosed have no known genetic link, suggesting a complex mix of causes.

What causes Parkinson’s Disease in most cases?

Parkinson’s Disease causes remain the focus of ongoing scientific research, but most experts agree that the condition results from a mix of genetic and environmental influences. The primary hallmark of the disease is the loss of dopamine-producing neurons in a region of the brain called the substantia nigra.This dopamine deficiency disrupts communication between the brain and muscles, leading to classic motor symptoms such as tremors, stiffness, and slowness of movement. Environmental exposures—such as certain pesticides or heavy metals—may increase the risk, particularly in individuals with a genetic predisposition.However, no single cause has been identified. Some cases are linked to genetic mutations, while others develop sporadically. Understanding these contributing factors can help researchers develop more targeted treatments and preventive strategies in the future.

Parkinson’s Disease: Signs, Struggles and Support

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What is Parkinson's Disease?

Parkinson’s Disease is a long-term neurological disorder that primarily affects movement. It develops when nerve cells in a specific region of the brain, known as the substantia nigra, are damaged or die. These cells produce dopamine, a chemical messenger that helps regulate movement, coordination, and other vital functions.

As dopamine levels decrease, individuals begin to experience difficulties with smooth and controlled movements. This condition is progressive, meaning Parkinson's Disease symptoms worsen over time.

But what causes Parkinson’s Disease? While the exact cause is not fully understood, researchers believe that a combination of genetic and environmental factors may contribute to its onset. The condition affects millions of people worldwide and typically begins after the age of 60, though younger individuals may also be diagnosed with early-onset Parkinson’s.

If you or a loved one is living withParkinson’s Disease, you're not alone. Recognizing the early signs of parkinson's symptoms and accessing the right support can make a meaningful difference.

Origins of Parkinson’s Disease

Parkinson’s Disease was first formally described in 1817 by British physician Dr. James Parkinson in his essay An Essay on the Shaking Palsy. He described key Parkinson's Disease symptoms like tremors, muscle rigidity, and slow movement, leading to the condition being named after him. However, historical records suggest similar Parkinson's symptoms were recognized as early as 5000 BCE in Ayurvedic medicine and in ancient Greek and Chinese texts.

Modern research has linked Parkinson’s Disease to dopamine deficiency and neuron degeneration in the brain's substantia nigra. While the exact cause remains unclear, scientists believe a combination of genetic and environmental factors contributes to its development. Ongoing research continues to uncover more about this complex condition.

For more details on the research, visit the Michael J. Fox Foundation's website: www.michaeljfox.org.

What causes Parkinson's Disease?

Loss of dopamine-producing neurons

Parkinson’s Disease develops when dopamine-producing nerve cells in the substantia nigra, a part of the brain responsible for movement control, gradually break down or die. Dopamine is essential for smooth and coordinated muscle movements. As its levels decrease, Parkinson's Disease symptoms, such as tremors, rigidity, and slow movement, begin to appear. Scientists are still investigating what triggers this neuron loss.

Environmental triggers

Exposure to environmental toxins has been linked to an increased risk of developing Parkinson’s Disease. Pesticides, herbicides, heavy metals, and industrial chemicals may contribute to nerve cell damage over time. Studies suggest that individuals who have long-term exposure to these substances, such as farmers, welders, or factory workers, may be at higher risk. However, not everyone exposed develops the disease, indicating that additional contributing factors are involved.

Genetic factors

Although most cases of Parkinson’s Disease are not inherited, about 10–15% are linked to genetic mutations. Specific genes, such as LRRK2, PARK7, PINK1, and SNCA, have been associated with an increased risk. While these mutations do not guarantee that someone will develop the disease, they play a role in its onset, particularly in early-onset Parkinson’s Disease cases

Eating with Parkinson's Disease

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Parkinson's Disease symptoms

Parkinson's Disease symptoms develop gradually and vary from person to person, often starting with subtle changes before progressing. The most common motor Parkinson's symptoms include:

Tremors, typically beginning in the hands or fingers
Bradykinesia (slowness of movement), making daily tasks difficult
Muscle rigidity causing stiffness and discomfort
Postural instability, leading to balance issues and increased risk of falls

In addition to movement-related Parkinson's Disease symptoms, many individuals experience non-motor challenges such as sleep disturbances, loss of smell, depression, cognitive impairment, and autonomic dysfunction (affecting blood pressure, digestion, and bladder control).

These Parkinson's symptoms worsen over time, impacting daily life, but early diagnosis and proper management can help improve mobility and overall well-being.

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Steadi-3 – Your Anti-Tremor Glove for Daily Independence

Steadiwear Inc

Steadi-3 – Your Anti-Tremor Glove for Daily Independence

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The Steadi-3 device for hand tremors offers practical support for individuals with Essential Tremors or Parkinson’s Disease. Designed to fit comfortably, it provides reliable, real-time tremor control tailored to the user’s needs, allowing for greater ease and independence.

Universal sizing: Our anti-tremor gloves are adjustable to meet your hand size. They are available for either hand and ensure an effective experience.
Compact, Comfortable Fit: With its silicone and Neoprene foam straps, the Steadi-3 Tremor glove is designed to fit securely without compromising comfort, allowing you to wear it throughout the day with ease.
Automatic Adjustment: The Steadi-3 adapts to your tremor intensity automatically, providing consistent stabilization as your tremor level changes in real time—functioning as an advanced hand stabilizer for tremors.
FDA-Registered for Safety: As an FDA-registered Class I medical device, the Steadi-3 glove is a trusted and safe choice among modern vibrating gloves for Parkinson's.

Slide your hand into the glove, ensuring it fits snugly around your palm.
Tighten the fit by adjusting the velcro until it feels securely in place but still comfortable.
Once the device is on, it will immediately calibrate itself to your tremor frequency, and starts stabilizing your hands

The Steadi-3 glove offers a simple, battery-free solution designed to provide immediate relief from hand tremors, helping you regain control over daily tasks with ease

Warranty: We back our product with a one-year warranty.
Risk-Free Trial: With our 30-day hassle-free return policy, you can test the Steadi-3 glove with confidence.
Regain Control: Combat hand tremors effectively with the trusted Steadi-3 anti-tremor glove from Steadiwear.

Please be aware that all returns are subject to a restocking fee of $83 USD or $117 CAD per unit to cover shipping, returns, customs and fulfillment. This fee will be deducted from your refund in the case of a return request.